Disease #05796 (CSS10 (Coffin-Siris syndrome, type 10 (CSS10)), OMIM:618506)

Official abbreviation CSS10
Name Coffin-Siris syndrome, type 10 (CSS10)
OMIM ID 618506
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene SOX4
Associated tissues -
Disease features -
Remarks -
Date created 2020-07-25 09:05:48 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00436401 269706 - - M no Germany - - - - - CSS10 Delayed speech and language development, Intellectual disability, borderline, Hypotonia, Patent foramen ovale, Pulmonic stenosis, Atypical behavior, Epicanthus, Wide nasal bridge, Long philtrum, Wide mouth, Sandal gap SOX4 SOX4 1 1 Andreas Laner
00448540 3bINP-001 PubMed: Vela-Amieva 2024 Incidental finding F no Mexico - - - - - CSS10 - - SOX4 1 1 Miriam Erandi Reyna-Fabián
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